Publications
- The coincidence of IgA nephropathy and Fabry disease2013 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Mutational Analysis of ACTN4, Encoding alpha-Actinin 4, in Patients with Focal Segmental Glomerulosclerosis Using HRM Method2013 | First Faculty of Medicine
- DNA Analysis of Renal Electrolyte Transporter Genes Among Patients Suffering from Bartter and Gitelman Syndromes - Summary of Mutation Screening2011 | First Faculty of Medicine
- New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease2009 | First Faculty of Medicine
- DNA analysis of autosomal dominant polycystic kidney disease in Czech Republic +12004 | First Faculty of Medicine
- DNA analysis in families with autosomal dominant polycystic kidney diseasePublication without faculty affiliation
- DNA analysis of polycystic kidney diseasePublication without faculty affiliation
- DNA analysis of autosomal dominant polycystic kidney disease in Czech families +2Publication without faculty affiliation
- The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Faculty of Medicine in Pilsen, Second Faculty of Medicine, Third Faculty of Medicine
- Current and Future Therapeutical Options in Alport Syndrome2023 | First Faculty of Medicine
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